Vikkula M - Search Results

1

Unravelling the molecular genetics of osteoarthrosis.

Vikkula M, Olsen BR. Vikkula M, et al. Ann Med. 1996 Aug;28(4):301-4. doi: 10.3109/07853899608999084. Ann Med. 1996. PMID: 8862683 Review.

2

Multiallelic polymorphism of the cartilage collagen gene: no association with osteoarthrosis.

Vikkula M, Nissilä M, Hirvensalo E, Nuotio P, Palotie A, Aho K, Peltonen L. Vikkula M, et al. Ann Rheum Dis. 1993 Oct;52(10):762-4. doi: 10.1136/ard.52.10.762. Ann Rheum Dis. 1993. PMID: 8257213 Free PMC article.

3

Type II collagen mutations in rare and common cartilage diseases.

Vikkula M, Metsäranta M, Ala-Kokko L. Vikkula M, et al. Ann Med. 1994 Apr;26(2):107-14. doi: 10.3109/07853899409147337. Ann Med. 1994. PMID: 8024727 Review.

4

Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus.

Vikkula M, Mariman EC, Lui VC, Zhidkova NI, Tiller GE, Goldring MB, van Beersum SE, de Waal Malefijt MC, van den Hoogen FH, Ropers HH, et al. Vikkula M, et al. Cell. 1995 Feb 10;80(3):431-7. doi: 10.1016/0092-8674(95)90493-x. Cell. 1995. PMID: 7859284

5

Assignment of a locus for dominantly inherited venous malformations to chromosome 9p.

Boon LM, Mulliken JB, Vikkula M, Watkins H, Seidman J, Olsen BR, Warman ML. Boon LM, et al. Among authors: vikkula m. Hum Mol Genet. 1994 Sep;3(9):1583-7. doi: 10.1093/hmg/3.9.1583. Hum Mol Genet. 1994. PMID: 7833915

6

The gene responsible for pseudohypoparathyroidism type Ib is paternally imprinted and maps in four unrelated kindreds to chromosome 20q13.3.

Jüppner H, Schipani E, Bastepe M, Cole DE, Lawson ML, Mannstadt M, Hendy GN, Plotkin H, Koshiyama H, Koh T, Crawford JD, Olsen BR, Vikkula M. Jüppner H, et al. Among authors: vikkula m. Proc Natl Acad Sci U S A. 1998 Sep 29;95(20):11798-803. doi: 10.1073/pnas.95.20.11798. Proc Natl Acad Sci U S A. 1998. PMID: 9751745 Free PMC article.

7

Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2.

Vikkula M, Boon LM, Carraway KL 3rd, Calvert JT, Diamonti AJ, Goumnerov B, Pasyk KA, Marchuk DA, Warman ML, Cantley LC, Mulliken JB, Olsen BR. Vikkula M, et al. Cell. 1996 Dec 27;87(7):1181-90. doi: 10.1016/s0092-8674(00)81814-0. Cell. 1996. PMID: 8980225

8

Predisposition to familial osteoarthrosis linked to type II collagen gene.

Palotie A, Väisänen P, Ott J, Ryhänen L, Elima K, Vikkula M, Cheah K, Vuorio E, Peltonen L. Palotie A, et al. Among authors: vikkula m. Lancet. 1989 Apr 29;1(8644):924-7. doi: 10.1016/s0140-6736(89)92507-5. Lancet. 1989. PMID: 2565419

9

Early-onset osteoarthritis linked to the type II procollagen gene. Detailed clinical phenotype and further analyses of the gene.

Vikkula M, Palotie A, Ritvaniemi P, Ott J, Ala-Kokko L, Sievers U, Aho K, Peltonen L. Vikkula M, et al. Arthritis Rheum. 1993 Mar;36(3):401-9. doi: 10.1002/art.1780360317. Arthritis Rheum. 1993. PMID: 8452585

10

Orofacial clefting: update on the role of genetics.

Ghassibe M, Bayet B, Revencu N, Desmyter L, Verellen-Dumoulin C, Gillerot Y, Deggouj N, Vanwijck R, Vikkula M; CL/P Study Group. Ghassibe M, et al. Among authors: vikkula m. B-ENT. 2006;2 Suppl 4:20-4. B-ENT. 2006. PMID: 17366841

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